Defoamer compositions containing organic particles

ABSTRACT

DEFOAMER COMPOSITIONS ARE PREPARED BY USING PARTICULAR OIL INSOLUBLE NORMALLY SOLID ORGANIC POLYMER PARTICLES, SECONDARY ORGANIC POLYMERS WHICH MAY BE OIL SOLUBLE OR OIL INSOLUBLE AND LIQUID HYDROCARBONS. OPTIONALLY, AMIDS AND SILICONE OILS ARE PRESENTS.

United States atent 3,697,440 Patented Oct. 10, 1972 3,697,440 DEFOAMER COMPOSITIONS CONTAINING ORGANIC PARTICLES Irwin A. Lichtman, Oradell, and Fred E. Woodward,

Watchung, N..ll., assignors to Diamond Shamrock Corporation, (Ileveland, Ohio No Drawing. Filed June 27,1969, Ser. No. 837,297 lint. Cl. B01d 17/00 US. Cl. 252-321 4 Claims ABSTRACT OF THE DISCLOSURE Defoamer compositions are prepared by using particular oil insoluble normally solid organic polymer particles, secondary organic polymers which may be oil soluble or oil insoluble and liquid hydrocarbons. Optionally, amides and silicone oils are present.

This invention relates to defoamer compositions and more particularly to novel defoamers containing particles of normally solid oil insoluble organic polymers.

It is an object of the present invention to provide novel dcfoamer compositions containing particular normally solid oil insoluble organic polymer particles, secondary organic polymers which may be oil soluble or oil insoluble and liquid hydrocarbons. It is another object to provide for novel defoaming processes using the aforementioned defoamer compositions. Other objects of this invention will become apparent from the detailed description given herein. However, it is intended that the detailed description and specific examples do not limit this invention but merely indicate preferred embodiments.

SUMMARY OF THE INVENTION The objects of this invention have been accomplished in the following manner. Defoamer compositions have been prepared by using particular normally solid oil insoluble organic polymer particles, secondary organic polymers which may be oil soluble or oil insoluble and liquid hydrocarbons. Optionally, amides and silicone oils are present. The compositions contain from about one to about 25 parts by weight of normally solid oil insoluble organic polymer particles, from about one to about 30 parts by weight of secondary organic polymers which may be oil soluble or oil insoluble, from about 50 to about 90 parts by weight of liquid hydrocarbon as the vehicle, from to about 25 parts by weight of normally solid amide and from 0 to about one part by weight of silicone oil.

These compositions are prepared by simple mixing of the components. For example, the oil soluble or oil insoluble secondary organic polymer and normally solid oil insoluble organic particles can be added to the liquid hydrocarbon vehicle. The normally solid amide, when used, is then added, the mixture homogenized and the silicone oil, when used, is added. Alternatively, the compositions can be prepared by heating together the normally solid oil insoluble organic particles, the secondary organic polymer, the amide, when used, and the liquid hydrocarbon vehicle provided that stabilizers are present in the normally solid polymer or added subsequently thereto. For example, if polyvinyl chloride particles are to be heated, the particles should contain any of the well known heat stabilizers for the polymer or else the stabilizers should be added to the system prior to heating.

The oil insoluble normally solid organic polymer Useful oil insoluble normally solid organic polymer particles, include both thermoplastic, thermosetting and naturally occurring polymers. Examples of thermoplastic polymers are polyvinyl chloride; polyvinylidene chloride;

polystyrene; polypropylene; high density polyethylene; polyamides, e.g., nylons; polyesters which are reaction products of dibasic acids, e.g., terephthalic acid, and glycols, e.g., hexamethylene glycol; cellulosics such as cellulose acetate, cellulose butyrate and purified cellulose; acrylics such as polymethyl methacrylate and polyethyl methacrylate; polyacrylonitrile and polyacrylamide. Copolymers are also useful. These are prepared by copolymerizing a monomer such as ethylene, propylene, styrene, vinyl chloride, acrylonitrile, etc. with a monoethylenically unsaturated monomer copolymerizable therewith. Such comonomer can itself be one of, e.g., ethylene, propylene, styrene, acrylonitrile, etc. Examples of such copolymers are the copolymer of ethylene and vinyl chloride and the copolymer of lauryl methacrylate and vinyl pyrrolidone in varying ratios of monomers.

Examples of thermosetting polymers are crosslinked polyesters, e.g., alkyd resins based on phthalic anhydride or maleic anhydride reacted with glycerine or any other polyester where either the acid or alcohol has more than two reactive groups; phenolic resins such as phenol-formaldehyde condensates, furfural-formaldehyde condensates and aminoplast resins such as urea-melamine resins and urea formaldehyde resins. Naturally occurring polymeric materials such as walnut shell ilour, proteins, e.g., collagen, and lignin derivatives such as sodium and ammonium lignin sulfonates are also suitable. It is preferred but not essential that such particles remain unsoftened at the temperature of the liquid whose foam is to be controlled. It is not necessary that such particles be waterinsoluble as well. These polymers can be used alone or in admixture with each other.

The size of these particles can vary widely. Particles can be as fine as 0.02 micron or less and as large as 200 mesh or greater. The finer size particles are preferred, e.g., from 0.02 to 0.2 micron. It is believed that the coarser particles, e.g., 200 mesh, are reduced in particle size during the homogenization step in the preparation of the defoarner.

The polymer particles useful herein can be prepared directly, can be produced by precipitation of polymers from polymer solutions, by grinding of polymer solids or the like. Methods for the preparation of these polymer particles are well known and this invention is not limited to any particular method of particle formation. The particle size requirements and preparation for the normally solid amide particles are the same as for the polymer particles.

The oil soluble or oil insoluble secondary polymer Examples of the oil soluble or oil insoluble secondary polymer are set forth below. An example of a secondary oil soluble organic polymer is a copolymer of vinyl acetate and fumaric acid esterified With a tallow alcohol and containing excess vinyl acetate. This material is available from Enjay Chemical Co. in the form of a mineral oil solution thereof under the trade name Pat-atone 440 which consists of about 25 parts by weight of copolymer in 75 parts by weight of a liquid hydrocarbon. This product has the following properties:

Viscosity at 210 F.," cs. 1300 Flash point, COC, F. 3 60 Color, ASTM 40 Specific gravity 60/60 F. 0.92

Other useful oil soluble polymers include vinyl acetate copolymerized with ethylenically unsaturated comonomers which are copolymerizable therewith such as maleic acid esters, ethylene, propylene and butylene; polyalkylene oxide adducts such as methyl glucoside propoxylated with four moles of propylene oxide; glycerine propoxylated with thirty moles of ethylene oxide and thirty moles of propylene oxide; the copolymer of lauryl methacrylate and vinyl pyrrolidone; blown vegetable oils such as blown hydrogenated soya oil, blown vegetable oil and blown castor oil; soya alkyds; phenol modified coumaroneindene resins; glycerol esters of gum rosin and polyvinylpyrrolidone, which is a solid but only partially oil soluble. These materials can be used alone or in admixture with each other.

It should be noted that in some instances, the oil insoluble normally solid organic polymers and the secondary oil soluble or oil insoluble organic polymers are interchangeable such as in the case of the copolymer of lauryl methacrylate and vinyl pyrrolidone. However, to practice the invention, the defoamer composition must contain both classes of polymers.

The liquid hydrocarbon vehicle The liquid hydrocarbon vehicle can be any liquid aliphatic, alicyclic, aromatic hydrocarbon. The hydrocarbon should be liquid at room temperature and atmospheric pressure, have a viscosity of from about 30 to about 400 SUS (Saybolt Universal Seconds at 100 F.), a minimum boiling point of at least 15 F. and an average from about 6 to 25 carbon atoms. Suitable hydrocarbons include hexane, heptane, octane, mineral seal oil, stoddard solvent, petroleum naphtha, benzene, toluene, xylene, parafiinic mineral oil, naphthenic mineral oil and the like. If desired, mixtures of two or more hydrocarbons can be used.

The normally solid amide Useful normally solid amides include those obtained by reaction of a polyamine containing at least one alkylene group having from two to six carbon atoms and a fatty acid having from six to eighteen carbon atoms. Generally, the polyamine and fatty acid are reacted together in stoichiometrically equivalent amounts. For example, the amide can be obtained by reaction of a polyamine with a fatty acid or mixture of fatty acids such as hexanoic, decanoic, lauric, palmitic, oleic and stearic acids, hydroxy acids such as ricinoleic acid or naphthenic acids obtained as byproducts in the refining of petroleum. Natural mixtures of fatty acids such as tall oil acids, tallow fatty acids and the like can be used. Suitable amines include ethylene diamine, butylene diamine, diethylene triamine, triethylene tetramine, hexamethylene diamine, decamethylene diamine, hydroxyethyl ethylene diamine, 1,3-diamine-2-propanol and the like.

An amide useful herein is hydrogenated tallow diamide of ethylene diamine. It was prepared by charging 95.7 parts by weight of bleached-hydrogenated tallow fatty acids into a stainless reactor equipped with condenser, water trap and agitator. The entire process including charging of reactants and cooling of the reaction product is carried out under a nitrogen atmosphere. The acids are then heated to about 165 C. to about 175 C. and 10.1 parts by weight of ethylene diamine is added. After the diamine is added, the reaction mixture is heated with agitation to about 180 C. to about 185 C. The mixture is reacted at about 180 C. to about 185 C. until the acid value is less than 5 and the alkalinity less than 0.6% by weight. The resulting reaction product of ethylene diamine and tallow fatty acid is then cooled to room temperature. If desired, the cooled reaction product can be ground to obtain the product in the form of a very fine powder. One or a mixture of amides can be used if desired.

The silicone oil The silicone oil can be a polysiloxane oil such as an alkyl, aryl, alicyclic or aralkyl siloxane or polysiloxane having a viscosity of from about 10 to about 3000 centistokes at 25 C. Preferred silicone oils include alkyl polysiloxanes having viscosities of from about 40 to about 1000 centistokes at 25 C. These alkyl polysiloxanes include dimethyl polysiloxane, diethyl polysiloxane, dipropyl polysiloxane, methyl ethyl polysiloxane, dioctyl polysiloxane, dihexyl polysiloxane, methyl propyl polysiloxane, dibutyl polysiloxane, didodecyl polysiloxane and the like, each having a viscosity of from about 10 to about 3000 centistokes at 25 C.

The defoamer compositions of this invention are especially adapted to defoam, i.e., inhibit formation of foam and destroy existing foam, in aqueous systems such as are found in the preparation of latex, glues, resinous materials, starches, paper pulp and the like. Defoamer compositions are used in small amounts depending upon the system in Which they are employed. In general, from about 0.01% to about 0.5% by weight of the defoamer based on the foam producing materials present in the aqueous system is satisfactory. Amounts in excess of about 0.5% by weight can be used to defoam aqueous systems but generally these amounts are not practical.

The defoamer compositions of Examples 1 through 43 and 45 through 51 were evaluated using the apparatus and procedure described below. A 1000 cc. tall form beaker is used. A curved glass outlet fused onto the base of the beaker is connected with a rubber hose to a centrifugal pump. The pump is used to circulate continuously the test liquid from the beaker into the pump and back into the beaker. Pumping is carried out at a rate so that the test liquid in the beaker is agitated by the re-entering test liquid to such an extent that foam forms. The pumping rate is about two gallons per minute. Test liquid enters the beaker at a point about 2.25 inches above the surface of the liquid in the beaker and strikes the surface of the liquid in the beaker at an angle of In carrying out the testing of the defoamer compositions, 500 cc. of concentrated pulping liquor containing about 0.5 tall oil soap is diluted 40:60 with water and charged at 180 F. into the beaker. This liquid, when quiescent at 180 F., fills the beaker to a level of about 3.25 inches from the bottom. This level is marked and labeled the 0 line. 0.1 cc. of defoamer composition is then added to the 500 cc. of test liquid in the beaker. Contents of the beaker are warmed to maintain the temperature at 180 F. during the test. The pump and stop watch are started simultaneously. Height of the foam above the 0 line is measured at 15 second intervals and recorded. An effective defoamer composition will maintain the height of the foam less than 3.15 inches above the 0 line for at least 60 seconds.

For a fuller understanding of the nature and objects of this invention, reference may be made to the following examples. These examples are given merely to illustrate the invention and are not to be construed in a limiting sense.

Where particle sizes of the normally solid polymer are not set forth in the examples, the material was reduced in size by grinding such that the resulting particles passed through a 300 mesh screen.

EXAMPLE 1 A defoamer composition was prepared by adding 10 parts by weight of Paratone 440 and 15 parts by weight of polyvinyl chloride particles to 71.8 parts by weight of mineral oil, then adding 3 parts by weight of amide, homogenizing in a Virtis 45 homogenizer and finally adding 0.2 parts by weight of 50 centistokes dimethyl polysiloxane oil.

The polyvinyl chloride was a plastisol grade identified as Opalon 440 (Monsanto Co.). The polyvinyl chloride content of the plastisol was greater than 98.5% While the soap content was about 1%. The product is supplied as a fine white powder having an average particle size less than one micron, a specific gravity of 1.40 and a specific viscosity of 054-057 (a solution of 0.40 grams of polymer in 100 m1. of cyclohexanone) The mineral oil was Parafiine Oil 372 (Gulf) and had the following properties:

Distillation range (1) Percent paraffinics 46 Percent naphthenics 43 Percent aromatics 11 Pour point -45 F. Flash point 345 F. Specific gravity, at 60 F. 0.9042 Viscosity, SUS, at 100 F. 100

Initial, 566 F.; 50% complete at 686 F. and end point at 818 F.

The amide was the hydrogenated tallow diamide of ethylene diamine obtained by reaction of hydrogenated tallow acids with ethylene diamine.

EXAMPLE 2 A defoamer composition was prepared by charging a vessel with 10 parts by weight of Paratone 440, 15 parts by weight of polyvinyl chloride particles having an average paritcle size of 0.5 micron and 71.2 parts by weight of mineral oil. 0.075 part by weight of each of two polyvinyl chloride stabilizers were added. One stabilizer was a mixed barium, cadmium, zinc salt of 2-ethyl hexanoic acid and the other was Drapex 6.8 (Argus Chem. Co.), an epoxy compound. At this point 2.0 parts by weight of hydrogenated tallow diamide of ethylene diamine was added, the mixture homogenized and then heated to 150 C. and held for 15 minutes at this temperature with vigorous stirring. The product was then cooled. 0.5 part by weight of a mixture of fatty amide and fatty esters and 1.0 part by weight of the aforesaid diamide were added. The mixture was homogenized, 0.20 part by weight of 50 centistoke dimethyl polysiloxane oil was added, and the mixture stirred.

EXAMPLE 3 Example 1 was repeated except that in place of the 10 parts by weight of Paratone 440, 10 parts by weight of blown soya oil was used.

Blown soya oil was prepared by bubbling air through refined soya bean oil at a temperature of 90 C., with agitation. This was continued until viscosity reached 1100 to 1200 seconds Saybolt Universal at 100 F.

EXAMPLE 4 Example 1 was repeated except that in place of the 10 parts by weight of Paratone 440, 10 parts of Unirez 628 was used.

Unirez 628 is the glycerol ester of gum rosin. The melting point by the ring and ball method is 9l96 C. The Gardner-Holdt viscosity of a 60% preparation in 38 KB mineral spirits is C-E. The acid number is 6-8 and the density in pounds/ gallon is 9.1 $0.1.

EXAMPLE Example 1 was repeated except that in place of the 10 parts by weight of Paratone 440, 10 parts by Weight of Elvax 150 was used.

Elvax (DuPont Co.) is a copolymer of vinyl acetate (32%-34%) and ethylene (66%68%). It is a medium viscosity resin with an inherent viscosity at 30 C. (0.25 g./100 ml. toluene) of 0.78. The density at 23 C. is

0.957 g./cc.

EXAMPLE 6 Example 1 was repeated except that in place of the 10 parts by weight of Paratone 440, 10 parts by weight of Elvax 250 was used.

Elvax 250 (DuPont Co.) is a copolymer of vinyl acetate (27%29% and ethylene (71%-73 It has an inherent viscosity at 30 C. (0.25 g./100 ml. toluene) of 0.85. The density at 23 C. is 0.951 g./ cc.

EXAMPLE 7 Example 1 was repeated except that in place of the 10 parts by weight of Paratone 440, 10 parts by weight of Elvax 310 was used.

Elvax 310 (DuPont Co.) is a copolymer of vinyl acetate (24%-26%) and ethylene (74%76%). It has an inherent viscosity at 30 C. (0.25 g./100 ml. toluene) of 0.54. The density at 23 C. is 0.949 g./cc.

EXAMPLE 8 Example 1 was repeated except that in place of the 10 parts by weight of Paratone 440, 10 parts by weight of Elvax 360 was used.

Elvax 360 (DuPont Co.) is a copolymer of vinyl acetate (24%-26%) and ethylene (74%76%). It has an inherent viscosity at 30 C. (0.25 g./100 ml. toluene) of 1.05. The density at 23 C. is 0.950 g./cc.

EXAMPLE 9 Example 1 was repeated except that in place of the 10 parts by weight of Paratone 440, 10 parts by weight of Dyal XAC-76 was used.

Dyal XAC-76 is a 64%66% medium soya oil alkyd in xylene solvent. Soya oil and glycerin are Twitchellized and reacted with phthalic anhydride. The Cure Value is 60-90 seconds, and the acid value is about 5.

EXAMPLE 10 Example 1 was repeated except that in place of the 10 parts by weight of Paratone 440, 10 parts by weight of polyoxypropylene glycol of approximate molecular Weight of 700 and having a hydroxyl number of was used. This material was made by reaction of butyl alcohol with propylene oxide.

EXAMPLE 11 EXAMPLE 12 Example 1 was repeated except that in place of the 10 parts by weight of Paratone 440, 10 parts by weight of Troykyd (Troy Chemical Co.) XYZ was used.

Troykyd XYZ is an alkyd prepared from partially hydrogenated vegetable oil.

EXAMPLE 13 Example 1 was repeated except that in place of the 10 parts by weight of Paratone 440, 10 parts by weight of Thanol 6500 was used.

Thanol 6500 (Jefferson Chem. Co.) is a polyol of glycerine, ethylene oxide and propylene oxide. The molecular weight is approximately 6500, and the hydroxyl number is about 25.

7 EXAMPLE 14 Example 1 was repeated except that in place of the parts by weight of Paratone 440, 10 parts by weight of Polyvinyl Pyrrolidone, Np-K30 (General Aniline and Film Co.) was used.

Polyvinyl Pyrrolidone NpK30 has an average molecular weight of 40,000.

EXAMPLE 15 Example 1 was repeated except that in place of the 10 parts by weight of Paratone 440, 10 parts by weight of Poly-G 3030PG (Olin Chemicals Div.) was used.

Poly-G 3030PG is an alkylene oxide adduct of glycerine having a molecular weight of about 3,000, a hydroxyl number of 54.7-57.5, an acid number of 0.1, and a specific gravity of 1.008 (/20 C.).

EXAMPLE 16 Example 1 was repeated except that in place of the 10 parts by weight of Paratone 440, 10 parts by weight of Poly-G 435 DM (Olin Chemicals Div.) Was used.

Poly-G 435 DM is a propylene oxide adduct of methyl glucoside having a hydroxyl number of 435, an acid number of 0.10, and a viscosity of 18,000 centipoises at C.

EXAMPLE 17 A defoamer composition was prepared as follows:

3.7 parts by weight of polypropylene were added to 50.2 parts by weight of paraffin oil and heated to 170 C. The polypropylene was Hercoflat PA-47l having an average particle size of 150 microns, melting point of 333 F., index of refraction of 1.5 and specific gravity of 0.9. Separately, 20.0 parts by weight of Paratone 440 were added to 20.0 parts of parafiin oil and heated to 80 C. The two mixtures were combined and cooled to 140 C. At this temperature 5.0 parts by weight of hydrogenated tallow diamide of ethylene diamine were added and the mixture stirred vigorously while cooling to room temperature. 0.5 parts by weight of 50 centistoke silicone oil (dimethyl polysiloxane) were added and the mixture stirred vigorously until it appeared homogeneous. At this point, the mixture was diluted 1:1 with paraffin oil.

EXAMPLE 18 Example 1 was repeated except that in place of the 15 parts by weight of polyvinyl chloride particles, 15 parts by weight of purified wood cellulose (Solka-Floc BNB-40, Brown Co.) was used. This purified wood cellulose has an average particle length of 76 microns, an average particle width of 19 microns and a moisture content of approximately 6%.

EXAMPLE 19' Example 1 was repeated except that in place of the 15 parts by weight of polyvinyl chloride particles, 15 parts by weight of walnut shell flour (Agrashell, Inc., WF-3A) was used.

Agrashell WF-3A has an average chemical analysis of 60% by weight cellulose, 24% by weight lignin, 10% by weight furfural (calculated as pentosan), 5% by weight cutin and 6.5% by weight methoxyl as principal components.

EXAMPLE 20 Example 1 was repeated except that in place of the 15 parts by weight of polyvinyl chloride particles, 15 parts by weight of Superlose (Stein-Hall Co.) was used.

Superlose is the amylose fraction of starch. It is a natural polymer having a molecular weight of about 150,000, a moisture content of 10% and an ash content of 0.5%. Superlose is chemically identical to cellulose, but has a coiled structure due to its alpha linkage, while the cellulose molecule is rigid.

8 EXAMPLE 21 EXAMPLE 22 Example 1 was repeated except that in place of the 15 parts by weight of polyvinyl chloride particles, 15 parts by weight of Elvacite 2042 (DuPont Co.) was used.

Elvacite 2042 is a very high molecular weight ethyl methacrylate polymer having an average inherent viscosity of 0.91 (as determined for a solution containing 0.25 g. polymer in 50 ml. chloroform at 25 C.).

Example 1 was repeated except that in place of the 15 par-ts by weight of polyvinyl chloride particles, 15 parts by weight of Elvacite 2045 (DuPont Co.) was used.

Elvacite 2045 is a high molecular weight isobutyl methacrylate polymer having an average inherent viscosity of 0.66 (as determined for a solution containing 0.25 g. polymer in 50 ml. chloroform at 25 C.). An inherent viscosity of 0.55 corresponds to an average molecular weight of about 300,000.

EXAMPLE 24 Example 1 was repeated except that in place of the 15 parts by weight of polyvinyl chloride particles, 15 parts by weight of Amberol ST-140-F (Rohm & Haas Co.) was added.

Amberol 'ST-140-F is a phenol-formaldehyde polymer having an acid number of 20-40 and an approximate specific gravity of 1.04. A 64% solids solution in toluol has a Gardner-Holdt bubble tube viscosity range of I-Q.

EXAMPLE 25 Example 1 was repeated except that in place of the 15 parts by weight of polyvinyl chloride particles, 15 parts by weight of Saran Resin F-310 (Dow Chemical Co.) was added.

Saran F3'1=0 resin is a copolymer of vinylidene chloride and acrylonitrile. The specific gravity 25/4 C. is 1.60. The viscosity of a 20% solution in methyl ethyl ketone is approximately centipoises.

EXAMPLE '26 Example 1 was repeated except that in place of the 15 parts by weight of polyvinyl chloride particles, 15 parts by weight of Orzan A (Crown Zellerbach Co.) was added.

'Orzan A is essentially ammonium lignin sulfonate plus wood sugars. It consists of 57% lignin sulfonic acids and 15% reducing sugars (calculated as glucose). Lignin is a wood polymer with an average molecular weight of about 10,000.

EXAMPLE 27 Example 1 was repeated except that in place of the 15 parts by weight of polyvinyl chloride particles, 15 parts by weight of Eastman EAB-l71-2 (Eastman Chemical Products) was added.

Eastman EAB17 1--2 is a cellulose acetate butyrate polymer containing an average of 1.5% hydroxyl, 29.5% acetal and 17% butyral radicals. The viscosity lies in the range 5.6-9.4 poises and the specific gravity is 1.25.

9 EXAMPLE 28 Example 1 was repeated except that in place of the 15 parts by weight of polyvinyl chloride particles, 15 parts by weight of Swifts Technical Protein Colloid 40 Mega Special was used.

Swifts Technical Protein Colloid 40 Mega Special is an extracted, highly refined, dry granular protein of collagen source. The digestible protein content is approximately 85%.

EXAMPLE 29 A defoamer composition was prepared by adding parts by weight of the glycerol ester of gum rosin (Unirez 628) and parts by weight of purified wood cellulose (Solka-Floc BNB-40) to 71.8 parts by weight of mineral oil. Then 3 parts by weight of the amide of Example 1 was added. The mixture was then homogenized'in a Virtis 45 homogenizer. After homogenizing, 0.2 parts by weight of 50 centistoke silicone oil (dimethylpolysiloxane) was added.

EXAMPLE 30 Example 29 was repeated except that in place of Unirez 628, 10 parts by weight of blown soya oil was added.

EXAMPLE 31 Example 29 was repeated except that in place of Unirez 628, 10 parts by weight of Elvax 150 was used.

EXAMPLE 32 A defoamer composition was prepared by adding 10 parts by weight of Unirez 628 and 15 parts by weight of Swifts Technical Protein Colloid 40 Mega Special to 71.8 parts by weight of mineral oil. Then 3 parts by weight of the amide of Example 1 was added. The mixture was then homogenized in a V-irtis 45 homogenizer. After homogenization, 0.2 parts by weight of 50 centistoke silicone oil (dimethyl polysiloxane) was added.

EXAMPLE 33 Example 32 was repeated except that in place of Unirez 628, 10 parts by weight of blown soya oil was used.

EXAMPLE 34 Example 32 was repeated except that in place of the Unirez 628, 10 parts by weight of Elvax 150 was used.

EXAMPLE 35 Example 1 was repeated except that in place of the 3 parts by weight of hydrogenated tallow diamide of ethylene diamine, 3 parts by weight of stearyl diamide of hexamethylene diamine was added.

EXAMP LE 36 A defoamer composition was prepared by adding 10 parts by weight of Nevillac 10 and 15 parts by weight of ammonium lignin sulfonate to 71.8 parts by weight of mineral oil. Then, 3 parts by weight of the amide of Example 1 was added and homogenizing in a Vitris 45 homogenizer was carried out. After homogenizing, 0.2 parts by weight of 50 centistoke silicone oil (dimethylpolysiloxane) was added.

EXAMPLE 37 Example 36 was repeated except that in place of ammonium lignin sulfonate, 15 parts by weight of Agrashell WE-3A was added.

EXAMPLE 38 Example 36 was followed except that in place of ammonium lignin sulfonate, 15 parts by weight of Eastman EAB1712 was added.

EXAMPLE 39 Example 36 was followed except that in place of ammonium lignin sulfonate, 15 parts by weight of Saran F-310 was used.

EXAMPLE 40 EXAMPLE 41 Example 40 was repeated except that in place of the Elvax 150, 3 parts by weight of Troykyd XYZ was added.

EXAMPLE 42 Example 40 was repeated except that in place of Elvax 150, 3 parts by weight of blown soya bean oil was added.

EXAMPLE 43 Example 40 was repeated except that in place of Elvax 150, 3 parts by weight of Unirex 628 was used.

EXAMPLE 45 Example 40 was repeated except that in place of Elvax 150, 3 parts by weight of blown soya oil were used, and the parafiin oil was replaced by mineral seal oil.

EXAMPLE 46 A defoamer composition was prepared by adding 25 parts by weight of Orzan A, 30 parts by weight of Elvax and 15 parts by weight of the amine of Example 1 to 29.8 parts by weight of paraffin oil and homogenizing on a Virtis 45 homogenizer. 0.20 part by weight of 50 centistoke silicone oil (dimethylpolysiloxane) were then added.

EXAMPLE 47 Example 46 was repeated except that in place of Elvax 150, 30 parts by weight of Troykyd XYZ was used.

EXAMPLE 48 Example 46 was repeated except that in place of Elvax 150, 30 parts by weight of blown soya bean oil was used.

EXAMPLE 49 Example 46 was repeated except that in place of Elvax 150, 30 parts by weight of Unitex 628 was used.

EXAMPLE 50 A defoamer composition was prepared by charging a vessel with 15 parts by weight of Opalon 440, 10 parts byweight of Paratone 440 and 74.5 parts by weight of paraffin oil. Two polyvinyl chloride stabilizers were added at 0.075 parts by weight of each, viz., a mixed barium, cadmium, zinc salt of Z-ethylhexanoic acid and Drapex 6.8 (Argus Chem. Co.) an epoxy compound. The mixture was homogenized, heated to 150 C. with stirring and held at that temperature for 15 minutes. It was then cooled to room temperature, homogenized and 0.2 parts by weight of 50 centistoke silicone oil (dimethylpolysiloxane) was added, and the mixture was stirred.

EXAMPLE 51 Example 50 was followed except the amount of parafi'in oil used was 74 parts by weight and 0.5 parts by weight of a mixture of fatty amides and fatty esters were added to the mixture just prior to the final homogenization period. The mixture of fatty amides and esters contained coco fatty acid alkalolamide, oleic amide and an oleic ester of polyglycol of molecular weight of about 600.

The compositions of Examples 1 through 51 were tested for their defoaming ability using the method and apparatus described above. The test data obtained is set forth in Table I.

11 TABLE 1 Time for foam to rise to 3.15

Composition of inch level above zero point Example- (seconds) 1 150 14 120 15 90 16 90 17 90 18 180 19 150 20 I 150 21 9O 22 90 23 120 24 90 25 90 26 150 27 120 28 150 29 120 30 120 31 120 32 120 33 120 34 180 35 120 36 90 37 120 38 180 39 i 90 40 90 41 90 42 120 43 90 45 120 46 90 47 90 48 90 49 90 50 90 51 90 Blank 20 The compositions of the following examples were evaluated using the following test method:

A 0.02% by weight solution in water of sodium dodecyl benzene sulfonate, a foam producing surfactant, was prepared. The surfactant was 46% active. A 200 cc. quantity of this solution, identified as the blank, was hand shaken in a 500 cc. Erlenmeyer flask in a reproducible manner. The foam reached a height of approximately one inch.

In conducting the evaluation, one drop of the defoamer composition to be tested was added to a freshly prepared 200 cc. quantity of test solution and the solution shaken in the same manner as done in the case of the blank. The presence of foam was observed and recorded.

EXAMPLE 52 A defoamer composition was prepared by adding 30 parts by weight of blown soya bean oil and 25 parts by weight of Orzan A to 29. 8 parts by weight of mineral seal oil, adding 15 parts by weight of the hydrogenated tallow diamide of ethylene diamine, homogenizing in a Virtis 45 homogenize'r and finally adding 0.2 part by weight of 50 centistoke silicone oil (dimethylpolysiloxane oil).

EXAMPLE 53 Example 52 was repeated except that in place of the blown soya oil, 30 parts by weight of Troykyd XYZ was added and in place of the mineral seal oil, 29.8 parts by weight of kerosene was added.

EXAMPLE 54 Example 52 was repeated except that in place of Orzan A, 25 parts by weight of Agrashell WF-3A was added, the amide was eliminated and the kerosene was increased to 44.8 parts by weight.

EXAMPLE 55 Example 52 was repeated except that in place of Orzan A, 25 parts by weight of Agrashell WF-7A was added, in place of the blown soya oil, 30 parts of Paratone 440 was added, the amide was eliminated and 44.8 parts by weight of paraffin oil was added.

EXAMPLE 56 Example 52 was repeated except that in place of the blown soya oil, 30 parts by weight of Thanol 6500 was added, in place of the Orzan A, 25 parts by weight of Protein Colloid 40 Mega Special was added, the amide component was eliminated and the mineral seal oil content adjusted to 44.8 parts by weight.

EXAMPLE 57 Example 52 was repeated except that in place of the blown soya oil, 30 parts by weight of Elvax was added, in place of the Orzan A, 25 parts by weight of Superlose was added, the amide component was eliminated and in place of mineral seal oil, 44.8 parts by weight of parafiin oil was added.

EXAMPLE 5 8 EXAMPLE 59 Example 58 was repeated except that in place of Troykyd XYZ, 30 parts by weight of Elvax 150 was added.

EXAMPLE 60 Example 58 was repeated except that in place of Troykyd XYZ, 30 parts by weight of blown soya oil was added.

EXAMPLE 61 Example 58 was repeated except that in place of Troykyd XYZ, 30 parts by weight of Unirez 628 was added.

EXAMPLE 62 A defoamer composition was prepared by adding 30 parts by weight of Troykyd XYZ and 25 parts by weight of Agrashell WF-3A to 41.2 parts by wt. mineral seal oil, adding 3 parts 'by weight of the oleyl diamide of hexamethylene diamine, homogenizing in a Virtis 45 homogenizer. No silicone oil was added.

13 EXAMPLE 63 Example 62 was repeated except in place of the Troykyd XYZ, 30 parts by weight of Elvax 150 was added and 41.2 parts by weight of parafi m oil was used in place of mineral seal oil.

EXAMPLE 64 Example 62 was repeated except that in place of the Troykyd XYZ, 30 parts by weight of blown soya oil was added.

EXAMPLE 65 Example 62 was repeated except that in place of the Troykyd XYZ, 30 parts by weight of Unirez 628 was added.

EXAMPLE 66 A defoamer composition was prepared by adding 3 parts by weight of Olin Poly-G 3030 PG and 5 parts by weight of Eastman EAB-l71-2 to 81.8 parts by weight of mineral oil, adding parts by weight of the stearyl diamide of hexarnethylene diamine, homogenizing in a Virtis 45 homogenizer and finally adding 0.2 part by weight of 50 centistoke silicone oil (dimethylpolysiloxane).

EXAMPLE 67 Example 66 was repeated except that in place of the Olin Poly-G 3030 PG, 3 parts by weight of Dyal XAC- 76 was added and a less naphthenic mineral oil was added.

The mineral oil used was Parafiine Oil 333 (Gulf) and had the following properties:

Example 66 was repeated except that in place of the Olin Poly-G 3030 PG, 3 parts by weight of polyvinyl pyrrolidone (Gen. Aniline and Film NP-K30) were added and 81.8 parts by weight of mineral seal oil were used in place of the mineral oil.

EXAMPLE 69 Example 66 was repeated except that in place of the Olin Poly-G 3030 PG, 3 parts by weight of Troykyd XYZ was added and 818 parts by weight of mineral seal oil were used in place or" mineral oil.

EXAMPLE 70 A defoamer composition was prepared by adding 3 parts by weight of Troykyd XYZ and 5 parts by weight of Orzan S to 81.8 parts by weight of mineral oil, adding 10 parts by weight of the stearyl diamide of hexamethylene diamine, homogenizing on a Virtis 45 homogenizer and finally adding 0.2 parts by weight of 50 centistoke silicone oil (dimethylpolysiloxane).

EXAMPLE 71 Example 70 was repeated except that in place of the Troykyd XYZ, 3 parts by weight of Elvax 150 was added.

EXAMPLE 72 Example 70 was repeated except that in place of the Troykyd XYZ, 3 parts by weight of blown soya oil was added.

EXAMPLE 73 The preparation method of Example 70 was repeated except that in place of the Troykyd XYZ, 3 parts by weight of Unirez 628 was added.

14 EXAMPLE 74 A defoamer composition was prepared by adding 3 parts by weight of Troykyd XYZ and 5 parts by weight of Swifts Protein Colloid 40 Mega Special to 81.8 parts by weight of Paraffine Oil 333 (Gulf Co.), adding 10 parts by weight of oleyl diamide of hexamethylene diamine, homogenizing in a Virtis 45 homogenizer and finally adding 0.2 parts by weight of 50 centistoke silicone oil dimethylpolysiloxane) EXAMPLE 75 Example 74 was repeated except that in place of the Troykyd XY Z, 3 parts by weight of Elvax 150 was added and 81.8 parts of Gulf Paraffine Oil 372 was added in place of Gulf Parafiine Oil 333.

EXAMPLE 76 Example 74 was followed except that in place of the Troykyd XYZ, 3 parts by Weight of blown soya oil was added.

EXAMPLE 77 Example 74 was repeated except that in place of the Troykyd XYZ, 3 parts by weight of Unirez 628 was added and 81.8 parts by weight of Gulf Parafiine Oil 372 was added in place of Gulf Paratfine Oil 333.

EXAMPLE 78 A defoamer composition was prepared by adding 3 parts by weight of Elvax 150 and 5 parts by weight of Solka-Floc BNB-40 to 91.8 parts by weight of Gulf Paraffine Oil 333, homogenizing in a Virtis 45 homogenizer and finally adding 0.2 parts by weight of 50 centistoke silicone oil (dimethylpolysiloxane) EXAMPLE 79 Example 78 was repeated except that 3 parts by weight of blown soya oil were added in place of the Elvax 150 and kerosene was used in place of Gulf Paraifine Oil 333.

EXAMPLE 80 Example 78 was repeated except that 3 parts by weight of Dyal XAC-76 were added in place of the Elvax 150 and mineral seal oil was used in place of the Gulf Paraffine Oil 333.

EXAMPLE 81 A defoamer composition was prepared by adding 5 parts by weight of Troykyd XYZ and 5 parts by weight of Eastman EAB1712 to 89.8 parts by weight of mineral seal oil, homogenizing in a Virtis 45 homogenizer and finally adding 0.2 parts by weight of 50 centistoke silicone oil (dimethylpolysiloxane).

EXAMPLE 82 Example 81 was repeated except that 5 parts by weight of Olin Poly-G 3030 PG were added in place of the Troykyd XYZ and Gulf Parafiine Oil 372 was used in place of mineral seal oil.

EXAMPLE 83 Example 81 was repeated except that 5 parts by weight of Unirez 628 were added in place of the Troykyd XYZ and Gulf Paraffine Oil 333 was used in place of mineral seal oil.

EXAMPLE 84 A de foamer composition was prepared by adding 5 parts by weight of Olin Poly-G 3030 PG and 5 parts by weight of Superlose to 90 parts by weight of mineral seal oil and homogenizing in a Virtis 45 homogenizer.

EXAMPLE 85 Example 84 was repeated except that 5 parts by weight of blown soya oil were added in place of the Olin Poly-G 3030 PG and Gulf Parafline Oil 372 was used in place of mineral seal oil.

1 5 EXAMPLE 86 A defoamer composition was prepared by adding 30 parts by weight of Unirez 628 and 25 parts by weight of Orzan S to 44.8 parts by weight of mineral seal oil, homogenizing in a Virtis 45 homogenizer and finally adding 0.2 parts by weight of 50 centistoke silicone oil (dimethylpolysiloxane) EXAMPLE 87 Example 86 was repeated except that 30 parts by weight of blown soya oil were added in place of the Unirez 628 and Gulf Paraifine Oil 333 was used in place of mineral seal oil.

EXAMPLE 88 Example 86 was repeated except that 30 parts by weight of Elvax 150 was added in place of Unirez 628 and Gulf Parafline Oil 333 was used in place of mineral seal oil.

EXAMPLE 89 A defoamer composition was prepared by addin 30 parts by weight of blown soya oil and 25 parts by weight of Agrashell WF-7A to 44.8 parts by weight of kerosene, homogenizing in a Virtis 45 homogenizer and finally adding 0.2 parts by weight of 50 centistoke silicone oil (dimethylpolysiloxane oil).

EXAMPLE 90 Example 89 was repeated except that 30 parts by weight of Unirez 628 were added in place of the blown soya oil and Gulf Paraffine Oil 333 was used in place of kerosene.

EXAMPLE 91 Example 89 was repeated except that 30 parts by weight of Dyal XAC-7 6 were added in place of the blown soya oil and mineral seal oil was used in place of kerosene.

EXAMPLE 92 A defoamer composition was prepared by adding 30 parts by weight of blown soya oil and 25 parts by weight of Swifts Technical Protein Colloid 40 Mega Special to 45 parts of mineral seal oil and homogenizing in a Virtis 45 homogenizer.

EXAMPLE 93 Example 92 was repeated except that 30 parts by weight of Dyal XAC-76 were added in place of the blown soya oil and Gulf Parafiine Oil 333 was used in place of mineral seal oil.

EXAMPLE 94 Example 92 was repeated except that 30 parts by weight of Olin Poly-G 3030 PG were added in place of the blown soya oil and Gulf Paraffine Oil 372 was used in place of mineral seal oil.

EXAMPLE 95 A defoamer composition was prepared by adding 30 parts by weight of blown soya oil and 25 parts by weight of Styron 678 (Dow Chemical Co.) to 45 parts by weight of Gulf Parafiine Oil 333 and homogenizing in a Virtis 45 homogenizer.

Styron 678 is a general purpose polystyrene having the following properties: specific gravity 1.04; melt viscosity 800 poises; Vicat softening point 194 F.

EXAMPLE 96 A defoamer composition was prepared by adding 6 parts by Weight of Paratone 440 and 5 parts by weight of Styron 678 to 78.8 parts by weight of Gulf Parafiine Oil 372, adding parts by weight of oleyl diamide of hexamethylene diamine, homogenizing on a Virtis 45 homogenizer and finally adding 0.2 part by weight of 350 centistoke silicone oil (dimethylpolysiloxane).

l 6 EXAMPLE 97 A defoamer composition was prepared by adding 5 parts by weight of Paratone 440 and 5 parts by Weight of Styron 678 to 79 parts by Weight of Gulf Parafiine Oil 333, adding 10 parts by weight of hydrogenated tallow diamide of ethylene diamine, homogenizing on a Virtis 45 homogenizer and finally adding 1.0 part by weight of centistoke silicone oil (dimethylpolysiloxane).

EXAMPLE 98 A defoamer composition was prepared by adding 5 parts by weight of blown soya oil and 5 parts by weight of Solka-Floc BNB-4O to 79.5 parts by weight of Gulf Paraffine Oil 372, adding 10 parts by weight of stearyl diamide of hexamethylene diamine, homogenizing in a Virtis 45 homogenizer and finally adding 0.5 part by weight of 500 centistoke silicone oil (dimethylpolysiloxane).

EXAMPLE 99 Example 98 was repeated except that in place of the blown soya oil, 5 parts by weight of Olin Poly-G 3030 PG were added, Gulf Parafiine Oil 372 was added in place of the Gulf Parafline Oil 333 and 0.5 part by weight of 10 centistoke silicone oil (dimethylpolysiloxane) was added in place of the 500 centistoke silicone oil.

EXAMPLE 100 A defoamer composition was prepared by adding 5 parts by weight of Paratone 440 and 5 parts by weight of Orzan S to 79.8 parts by weight of mineral seal oil, adding 10 parts by weight of oleyl diamide of hexamethylene diamine, homogenizing on a Virtis 45 homogenizer and finally adding 0.2 parts by weight of 1,000 centistoke silicone oil (dimethylpolysiloxane).

EXAMPLE 101 A defoamer composition was prepared by adding 30' parts by Weight of blown soya oil and 25 parts by weight of Orzan S to 41.8 parts by weight of Gulf Paraffine Oil 333, adding 3 parts by weight of stearyl diamide of hexamethylene diamine, homogenizing on a Virtis 45 homogenizer, and finally adding 0.2 parts by weight of 10 centistoke silicone oil (dimethylpolysiloxane).

EXAMPLE 102 A defoamer composition was prepared by adding 30 parts by weight of Paratone 440' and 25 parts by weight of Eastman EAB-171-2 to 43.8 parts by weight of mineral seal oil, adding 1 part by weight of oleyl diamide of hexamethylene diamine, homogenizing on a Virtis 45 homogenizer and finally adding 0.2 parts by weight of 500 centistoke silicone oil (dimethylpolysiloxane).

EXAMPLE 103 A defoamer composition was prepared by adding 30 parts by weight of blown soya oil and 25 parts by weight of Eastman EAB-l7l-2 to 43.5 parts by weight of Gulf Parafiine Oil 333, adding 1 part by weight of hydrogenated tallow diamide of ethylene diamine, homogenizing on a Virtis 45 homogenizer and finally adding 0.5 parts by weight of 350 centistoke silicone oil (dimethylpolysiloxane).

EXAMPLE 104 17 18 using the aforedescribed sodium dodecyl benzene sulfonate styrene, polypropylene, high density polyethylene, solution. nylon, terephthalic acidhexamethylene glycol poly- TABLE II esters, cellulose acetate, cellulose butyrate, purified Composition of Example- Foam height cellulose, polymethyl methacrylate, polyethyl meth- 1 No foam acrylate, polyacrylonitrile, polyacrylamide, the c- 52 D0 polymer of ethylene and vinyl chloride, the co olymer of lauryl methacrylate and vinyl pyrrolidone, an

22 fig gigf alkyd resin based on phthalic anhydride reacted with 55 Do. glycerine, an alkyd resin based on maleic anhydride 56 reacted with glycerine, phenol-formaldehyde con- 57 m 05 inch foam densates, furfural-formaldehyde condensates, urea- 58 m 0.25 inch foam melamine resins, urea-formaldehyde resins, walnut 59 Slight foam shellfiour, collagen, sodium lignin sulfonate, and am- 60 'I' No foam moniurn lignin sulfonate; 61 Do. (b) rom about 1 to about 30 parts by weight of second- 62 m 0.5 inch foam ary oil soluble or 011 insoluble organic polymers 63 Do selected from at least one of the group consisting of 64 No f the copolymer of vinyl acetate and fumaric acid 65 esterified with a tallow alcohol, the copolymer of 66 vinyl acetate with maleic and esters, the co olymer 67 D0 of vinyl acetate with ethylene, the copolymer of vinyl 68 Do. acetate with propylene, the copolymer of vinylacetate 69 Do. with butylene, methyl glucoside alkoxylated with four 70 moles of propylene oxide, glycerine alkoxylated with 71 thirty moles of ethylene oxide and thirty moles of 72 propylene oxide, the copolymer of lauryl methacrylate 73 Do. and vinyl pyrrolidone, blown hydrogenated soya oil, 74 blown vegetable oil, blown castor 011, soya alkyds, 75 Do. phenol modified coumaroneindene resins, glycerol 76 esters of gum rosin, glycerine esters of polyvinylpyr- 77 t r rolidone, and mixtures of the above, with the pro- 78 i viso that the polymers of (a) and (b) are different 7 0,25 inch foam, in a given composition; 0 (0) from about 50 to about 90 parts by weight of a 81 No f hydrocarbon vehicle having a viscosity of from about 2 30 to about 400 Saybolt Universal Seconds at 100 83 D F. and a minimum boiling point of at least 150 F.; 4 D (d) from 0 to about 25 parts by weight of normally 85 0.5 inch foam, solld amide which is the reaction product of a poly- 86 No foam, amine containing at least one alkylene group having 87 0.5 inch foam. from 2 to 6 carbon atoms and fatty acid having from 88 0,75 inch fo 6 to 18 carbon atoms; and 89 No foam, (e) from 0 to about 1 part by weight of silicon oil. 90 Do, 2. The method of claim 1 wherein from about 0.1% 91 D to about 0.5% by weight of said composition is added 92 0.25 inch foam. based on the weight of the foam producing materials pres- 93 Sli ht foam. ent in said aqueous system. 94 0.5 inch foam. 3. The method of claim 1 wherein said thermoplastic 95 No foam. polymer is polyvinylchloride. 96 Do. 4. A method according to claim 1 in which the nor- 97 Do. mally solid amide and silicone oil are present. 98 Do. 99 D References Cited 100 UNITED STATES PATENTS 101 2,440,489 4/1948 Rosen et a1. 252 3z1 102 2,727,009 12/1955 Jorisch 252 321 103 2,820,696 1/l958 Morris 252-32 104 3,313,736 4/1967 Dickson et al. z52 321 What is claimed is: 3,334,147 8/1967 Brunelle et al. 252321 1. A method of defoaming aqueous systems which con- 3,336,231 8/1967 Marsh et al. 252321 sists essentially of adding to said aqueous systems a foam 2,751,358 6/ 1956 Caviet 252-358 controlling amount of a defoamer composition consisting 3,127,352 3/1964 Starke, Jr., et a1. 252-358 essentially of 3,388,072 6/1968 Domba 252321 (a) from about 1 to about 25 parts by weight of oil insoluble organic polymers, which are solid at the JOHN D. WELSH, Primary Examiner temperature of the aqueous system to be defoarned, selected from at least one of the group consisting of polyvinyl chloride, polyvinylidene chloride, poly- 252-358 UNITED STATES PATENT AND TRADEMARK OFFICE CERTIFICATE OF CORRECTION PATENT NO. 3,697, r ro DATED October 10 l972 |NV ENTOR(S) I rwin A. Lichtman and Fred E Woodward It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:

Column 3, l ine 33, 'l5" should be --l50--. Column 3 l ine 67, after "stainless" insert --steel Column 5 l ine 35, "pari tcle" should be --part i cle-- Column l0, l ine +8, "Uni tex" should be --Uni rez-. Column 13, line 40, "percent at 720F" should be 50 0 at 720F--. Column l8, l ine +3, "si l icon" should be -si l icone" Signed and Scaled this Arrest:

RUTH C. MASON C. MARSHALL DANN Arresting Officer Commissioner of Parents and Trademarks UNITED STATES PATENT AND TRADEMARK OFFICE CERTIFICATE OF CORRECTION PATENT NO. 3,697, i r0 DATED I October l0 l972 lN\/ ENTOR(S) l rwin A. Lichtman and Fred E Woodward It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:

Column 3, l ine 38, "l5 should be --l50--. Column 3, l ine 67, after "stainless" insert "steel". Column 5, line 35, "paritcle" should-be -particle--. Column l0, line &8, "Unitex" should be --Unirez--. Column 1 3, l ine iO "percent at 720F" should be "50% at 720F-- Column l8, line +3, "silicon" should be --silicone--.

* Signed and Scaled this Twenty-sixth Day of October 1976 [SEAL] Arrest.-

RUTH C. MASON C. MARSHALL DANN 8 ff Commissioner ojParenrs and Trademarks 

